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Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type Maroteaux

Crossref DOI link: https://doi.org/10.1016/j.biocel.2018.07.004

Published Print: 2018-09

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Irfanullah,

Zeb, Amir

Shinwari, Naila

Shah, Khadim

Gilani, Syed Zohaib Tayyab

Khan, Saadullah

Lee, Keun Woo

Raza, Syed Irfan

Hussain, Shabir

Liaqat, Khurram

Ahmad, Wasim https://orcid.org/0000-0003-1541-7258
Funding

Funding for this research was provided by:

Higher Education Commission (HEC), Islamabad, Pakistan

HEC-Indigenous PhD scholarships
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Text and Data Mining valid from 2018-09-01

Text and Data Mining valid from 2018-09-01
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This article is maintained by: Elsevier

Article Title: Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type Maroteaux

Journal Title: The International Journal of Biochemistry & Cell Biology

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.biocel.2018.07.004

Content Type: article

Copyright: © 2018 Published by Elsevier Ltd.

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